lubimin
spiro(4.5)decane-6-carboxaldehyde, 8-hydroxy-10-methyl-2-(1-methylethenyl)-, (5S-(5alpha(S*),6beta,8beta,10beta))-
 
Notes:
Stress product from potato tubers
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CAS Number: 35951-50-9Picture of molecule3D/inchi
XlogP3-AA: 3.40 (est)
Molecular Weight: 236.35468000
Formula: C15 H24 O2
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 352.05 °C. @ 760.00 mm Hg (est)
Flash Point: 302.00 °F. TCC ( 150.00 °C. ) (est)
logP (o/w): 3.224 (est)
Soluble in:
 water, 32.04 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
 None found
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Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: natural substances and extractives
Recommendation for lubimin usage levels up to:
 not for fragrance use.
 
Recommendation for lubimin flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
Cancer Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 160255
National Institute of Allergy and Infectious Diseases: Data
 (3R,6R,8S,10S)-8-hydroxy-6-methyl-3-prop-1-en-2-ylspiro[4.5]decane-10-carbaldehyde
Chemidplus: 0035951509
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References:
 (3R,6R,8S,10S)-8-hydroxy-6-methyl-3-prop-1-en-2-ylspiro[4.5]decane-10-carbaldehyde
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 160255
Pubchem (sid): 135115788
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
KEGG (GenomeNet): C09700
HMDB (The Human Metabolome Database): HMDB35032
FooDB: FDB014318
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 eggplant plant
Search Trop  Picture
 potato tuber
Search Trop  Picture
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Synonyms:
(5S-(5alpha(S*),6beta,8beta,10beta))-8-hydroxy-10-methyl-2-(1-methyl ethenyl) spiro(4.5)decane-6-carboxaldehyde
(3R,6R,8S,10S)-8-hydroxy-6-methyl-3-prop-1-en-2-ylspiro[4.5]decane-10-carbaldehyde
 spiro(4.5)decane-6-carboxaldehyde, 8-hydroxy-10-methyl-2-(1-methylethenyl)-, (5S-(5alpha(S*),6beta,8beta,10beta))-
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Articles:
PubMed: Multi-platform metabolomic analyses of ergosterol-induced dynamic changes in Nicotiana tabacum cells.
PubMed: Ergosterol-induced sesquiterpenoid synthesis in tobacco cells.
PubMed: Anti-fungal sesquiterpenoid from the root exudate of Solanum abutiloides.
PubMed: Enhanced production of antimicrobial sesquiterpenes and lipoxygenase metabolites in elicitor-treated hairy root cultures of Solanum tuberosum.
PubMed: Effect of elicitation on growth, respiration, and nutrient uptake of root and cell suspension cultures of Hyoscyamus muticus.
PubMed: An ATP-binding cassette multidrug-resistance transporter is necessary for tolerance of Gibberella pulicaris to phytoalexins and virulence on potato tubers.
PubMed: Sesquiterpenoids in root exudates of Solanum aethiopicum.
PubMed: Structural confirmation of 15-norlubiminol and 15-norepilubiminol, isolated from Solanum aethiopicum, by chemical conversion from lubimin and epilubimin, and their antifungal activity.
PubMed: Induction of plant gp91 phox homolog by fungal cell wall, arachidonic acid, and salicylic acid in potato.
PubMed: Sesquiterpenoids from the roots of Solanum aethiopicum.
PubMed: Induction of a polyubiquitin gene (ubi1) by potato phytoalexins and heat shock in Gibberella pulicaris.
PubMed: Phytoalexins from hairy roots of Hyoscyamus albus treated with methyl jasmonate.
PubMed: Novel study on the elicitation of hypersensitive response by polyunsaturated fatty acids in potato tuber.
PubMed: Abiotic factors elicit sesquiterpenoid phytoalexin production but not alkaloid production in transformed root cultures of Datura stramonium.
PubMed: Studies on the biosynthesis and metabolism of the phytoalexin lubimin and related compounds in Datura stramonium L.
PubMed: A role for ca in the elicitation of rishitin and lubimin accumulation in potato tuber tissue.
PubMed: Involvement of 3-hydroxy-3-methylglutaryl coenzyme a reductase in the regulation of sesquiterpenoid phytoalexin synthesis in potato.
PubMed: The effect of the phytoalexins, lubimin, (-)-maackiain, pinosylvin, and the related compounds dehydroloroglossol and hordatine M on human lymphoblastoid cell lines.
PubMed: Biotransformation of potato stress metabolites rishitin, lubimin, and 15-dihydro lubimin by potato and soybean cell cultures.
PubMed: Arachidonic acid-related elicitors of the hypersensitive response in potato and enhancement of their activities by glucans from Phytophthora infestans (Mont.) deBary.
PubMed: Effects of Controlled Atmospheres on Production of Sesquiterpenoid Stress Metabolites by White Potato Tuber: Possible Involvement of Cyanide-resistant Respiration.
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